ReP USP - Resultado da busca

Tese (Doutorado)
Diversification and species limits in two genera of the tribe Oryzomyini (Rodentia: Cricetidae: Sigmodontinae) revealed by combined molecular and cytogenetic approaches (2018)
Di-Nizo, Camilla Bruno; Silva, Maria José de Jesus (Orientador)
Unidade: IB
Subjects: CITOGENÉTICA MOLECULAR, CITOTAXONOMIA, MARCADOR MOLECULAR, FILOGENIA, ROEDORES, EVOLUÇÃO
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ABNT
DI-NIZO, Camilla Bruno. Diversification and species limits in two genera of the tribe Oryzomyini (Rodentia: Cricetidae. 2018. Tese (Doutorado) – Universidade de São Paulo, São Paulo, 2018. Disponível em: http://www.teses.usp.br/teses/disponiveis/41/41131/tde-26062018-084004/. Acesso em: 05 nov. 2024.
APA
Di-Nizo, C. B. (2018). Diversification and species limits in two genera of the tribe Oryzomyini (Rodentia: Cricetidae: Sigmodontinae) revealed by combined molecular and cytogenetic approaches (Tese (Doutorado). Universidade de São Paulo, São Paulo. Recuperado de http://www.teses.usp.br/teses/disponiveis/41/41131/tde-26062018-084004/
NLM
Di-Nizo CB. Diversification and species limits in two genera of the tribe Oryzomyini (Rodentia: Cricetidae: Sigmodontinae) revealed by combined molecular and cytogenetic approaches [Internet]. 2018 ;[citado 2024 nov. 05 ] Available from: http://www.teses.usp.br/teses/disponiveis/41/41131/tde-26062018-084004/
Vancouver
Di-Nizo CB. Diversification and species limits in two genera of the tribe Oryzomyini (Rodentia: Cricetidae: Sigmodontinae) revealed by combined molecular and cytogenetic approaches [Internet]. 2018 ;[citado 2024 nov. 05 ] Available from: http://www.teses.usp.br/teses/disponiveis/41/41131/tde-26062018-084004/
Artigo de periodico
Molecular cytogenetics and quality control: clinical guardians for pluripotent stem cells (2018)
Rohani, Leili; Johnson, Adiv A; Naghsh, Pooyan; Rancourt, Derrick E; Ulrich, Henning ; Holland, Heidrun
Source: Stem Cells Translational Medicine. Unidade: IQ
Subjects: CITOGENÉTICA MOLECULAR, CÉLULAS-TRONCO
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ABNT
ROHANI, Leili et al. Molecular cytogenetics and quality control: clinical guardians for pluripotent stem cells. Stem Cells Translational Medicine, p. 867-875, 2018Tradução . . Disponível em: https://doi.org/10.1002/sctm.18-0087. Acesso em: 05 nov. 2024.
APA
Rohani, L., Johnson, A. A., Naghsh, P., Rancourt, D. E., Ulrich, H., & Holland, H. (2018). Molecular cytogenetics and quality control: clinical guardians for pluripotent stem cells. Stem Cells Translational Medicine, 867-875. doi:10.1002/sctm.18-0087
NLM
Rohani L, Johnson AA, Naghsh P, Rancourt DE, Ulrich H, Holland H. Molecular cytogenetics and quality control: clinical guardians for pluripotent stem cells [Internet]. Stem Cells Translational Medicine. 2018 ; 867-875.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1002/sctm.18-0087
Vancouver
Rohani L, Johnson AA, Naghsh P, Rancourt DE, Ulrich H, Holland H. Molecular cytogenetics and quality control: clinical guardians for pluripotent stem cells [Internet]. Stem Cells Translational Medicine. 2018 ; 867-875.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1002/sctm.18-0087
Trabalho de evento-resumo
Evaluation of the functional consequence of SF1 overexpression in human cells (2018)
Pereira, Illy Enne Gomes; Rocha, Viviana Loureiro; Bidoia, Guilherme Brussolo; Gonçalves, Isabella Barbutti; Machado, João Agostinho; Traina, Fabiola; Saad, Sara Teresinha Olalla; Archangelo, Leticia Fröhlich
Source: Abstracts. Conference titles: Congress of The Brazilian Society for Cell Biology. Unidade: FMRP
Subjects: CITOGENÉTICA MOLECULAR, GENÉTICA MÉDICA
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ABNT
PEREIRA, Illy Enne Gomes et al. Evaluation of the functional consequence of SF1 overexpression in human cells. 2018, Anais.. São Paulo: SBBC, 2018. Disponível em: http://www.sbbc.org.br/wp-content/uploads/2014/08/Livro-ResumosSBBC2018.pdf. Acesso em: 05 nov. 2024.
APA
Pereira, I. E. G., Rocha, V. L., Bidoia, G. B., Gonçalves, I. B., Machado, J. A., Traina, F., et al. (2018). Evaluation of the functional consequence of SF1 overexpression in human cells. In Abstracts. São Paulo: SBBC. Recuperado de http://www.sbbc.org.br/wp-content/uploads/2014/08/Livro-ResumosSBBC2018.pdf
NLM
Pereira IEG, Rocha VL, Bidoia GB, Gonçalves IB, Machado JA, Traina F, Saad STO, Archangelo LF. Evaluation of the functional consequence of SF1 overexpression in human cells [Internet]. Abstracts. 2018 ;[citado 2024 nov. 05 ] Available from: http://www.sbbc.org.br/wp-content/uploads/2014/08/Livro-ResumosSBBC2018.pdf
Vancouver
Pereira IEG, Rocha VL, Bidoia GB, Gonçalves IB, Machado JA, Traina F, Saad STO, Archangelo LF. Evaluation of the functional consequence of SF1 overexpression in human cells [Internet]. Abstracts. 2018 ;[citado 2024 nov. 05 ] Available from: http://www.sbbc.org.br/wp-content/uploads/2014/08/Livro-ResumosSBBC2018.pdf
Artigo de periodico
A fast method to reprogram and CRISPR/Cas9 gene editing from erythroblasts (2018)
Melo, Uirá Souto; Leite, Felipe de Souza; Costa, Silvia; Rosenberg, Carla ; Zatz, Mayana
Source: Stem Cell Research. Unidade: IB
Subjects: CÉLULAS-TRONCO, GENÉTICA MÉDICA, CITOGENÉTICA MOLECULAR, MUTAÇÃO GENÉTICA, GENOMAS
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ABNT
MELO, Uirá Souto et al. A fast method to reprogram and CRISPR/Cas9 gene editing from erythroblasts. Stem Cell Research, v. 31, p. 52-54, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.scr.2018.07.002. Acesso em: 05 nov. 2024.
APA
Melo, U. S., Leite, F. de S., Costa, S., Rosenberg, C., & Zatz, M. (2018). A fast method to reprogram and CRISPR/Cas9 gene editing from erythroblasts. Stem Cell Research, 31, 52-54. doi:10.1016/j.scr.2018.07.002
NLM
Melo US, Leite F de S, Costa S, Rosenberg C, Zatz M. A fast method to reprogram and CRISPR/Cas9 gene editing from erythroblasts [Internet]. Stem Cell Research. 2018 ; 31 52-54.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1016/j.scr.2018.07.002
Vancouver
Melo US, Leite F de S, Costa S, Rosenberg C, Zatz M. A fast method to reprogram and CRISPR/Cas9 gene editing from erythroblasts [Internet]. Stem Cell Research. 2018 ; 31 52-54.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1016/j.scr.2018.07.002
Tese (Doutorado)
Characterization of chaotic genomic rearrangements in osteosarcoma (2018)
Gomes, Alexandra Galvão; Squire, Jeremy A (Orientador)
Unidade: FMRP
Subjects: OSTEOSSARCOMA, CITOGENÉTICA MOLECULAR
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ABNT
GOMES, Alexandra Galvão. Characterization of chaotic genomic rearrangements in osteosarcoma. 2018. Tese (Doutorado) – Universidade de São Paulo, Ribeirão Preto, 2018. Disponível em: https://www.teses.usp.br/teses/disponiveis/17/17135/tde-14052020-090705/. Acesso em: 05 nov. 2024.
APA
Gomes, A. G. (2018). Characterization of chaotic genomic rearrangements in osteosarcoma (Tese (Doutorado). Universidade de São Paulo, Ribeirão Preto. Recuperado de https://www.teses.usp.br/teses/disponiveis/17/17135/tde-14052020-090705/
NLM
Gomes AG. Characterization of chaotic genomic rearrangements in osteosarcoma [Internet]. 2018 ;[citado 2024 nov. 05 ] Available from: https://www.teses.usp.br/teses/disponiveis/17/17135/tde-14052020-090705/
Vancouver
Gomes AG. Characterization of chaotic genomic rearrangements in osteosarcoma [Internet]. 2018 ;[citado 2024 nov. 05 ] Available from: https://www.teses.usp.br/teses/disponiveis/17/17135/tde-14052020-090705/
Trabalho de evento-resumo
Familial non-disjunction and segregation variation of a supernumerary marker chromosome 15 in members of a large family (2017)
Joaquim, T. M.; Souza, D. C. de; Grangeiro, C. H. P.; Huber, Jair; Laus, Ana Carolina; Laureano, L. A. F.; Squire, Jeremy Andrew; Martelli, Lúcia Regina
Source: Abstracts. Conference titles: European Human Genetics Conference. Unidade: FMRP
Subjects: BIOMARCADORES, CROMOSSOMOS, GENÉTICA MÉDICA, CITOGENÉTICA MOLECULAR
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ABNT
JOAQUIM, T. M. et al. Familial non-disjunction and segregation variation of a supernumerary marker chromosome 15 in members of a large family. 2017, Anais.. Copenhagen: ESHG, 2017. . Acesso em: 05 nov. 2024.
APA
Joaquim, T. M., Souza, D. C. de, Grangeiro, C. H. P., Huber, J., Laus, A. C., Laureano, L. A. F., et al. (2017). Familial non-disjunction and segregation variation of a supernumerary marker chromosome 15 in members of a large family. In Abstracts. Copenhagen: ESHG.
NLM
Joaquim TM, Souza DC de, Grangeiro CHP, Huber J, Laus AC, Laureano LAF, Squire JA, Martelli LR. Familial non-disjunction and segregation variation of a supernumerary marker chromosome 15 in members of a large family. Abstracts. 2017 ;[citado 2024 nov. 05 ]
Vancouver
Joaquim TM, Souza DC de, Grangeiro CHP, Huber J, Laus AC, Laureano LAF, Squire JA, Martelli LR. Familial non-disjunction and segregation variation of a supernumerary marker chromosome 15 in members of a large family. Abstracts. 2017 ;[citado 2024 nov. 05 ]
Artigo de periodico
Efficient detection of chromosome imbalances and single nucleotide variants using targeted sequencing in the clinical setting (2017)
Villela, Darine; Costa, Silvia Souza; Vianna-Morgante, Angela M ; Krepischi, Ana Cristina Victorino ; Rosenberg, Carla
Source: European Journal of Medical Genetics. Unidade: IB
Subjects: CITOGENÉTICA MOLECULAR, SEQUÊNCIA DO DNA, GENOMAS, ANORMALIDADES CROMOSSÔMICAS, NUCLEOTÍDEOS
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ABNT
VILLELA, Darine et al. Efficient detection of chromosome imbalances and single nucleotide variants using targeted sequencing in the clinical setting. European Journal of Medical Genetics, v. 60, n. 12, p. 667-674, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.ejmg.2017.08.020. Acesso em: 05 nov. 2024.
APA
Villela, D., Costa, S. S., Vianna-Morgante, A. M., Krepischi, A. C. V., & Rosenberg, C. (2017). Efficient detection of chromosome imbalances and single nucleotide variants using targeted sequencing in the clinical setting. European Journal of Medical Genetics, 60( 12), 667-674. doi:10.1016/j.ejmg.2017.08.020
NLM
Villela D, Costa SS, Vianna-Morgante AM, Krepischi ACV, Rosenberg C. Efficient detection of chromosome imbalances and single nucleotide variants using targeted sequencing in the clinical setting [Internet]. European Journal of Medical Genetics. 2017 ; 60( 12): 667-674.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1016/j.ejmg.2017.08.020
Vancouver
Villela D, Costa SS, Vianna-Morgante AM, Krepischi ACV, Rosenberg C. Efficient detection of chromosome imbalances and single nucleotide variants using targeted sequencing in the clinical setting [Internet]. European Journal of Medical Genetics. 2017 ; 60( 12): 667-674.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1016/j.ejmg.2017.08.020
Trabalho de evento-resumo
Prevalence of skewed X chromosome inactivation pattern in a group of mosaic turner syndrome patients (2016)
Ruiz-Lara, G. V.; Luchiari, H. R.; Galerani, M. V.; Huber, Jair; Machado, F. B.; Ramos, Ester Silveira
Source: Abstracts. Conference titles: Workshop de Pós-Graduação em Genética. Unidade: FMRP
Subjects: CITOGENÉTICA MOLECULAR, CROMOSSOMO X
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ABNT
RUIZ-LARA, G. V. et al. Prevalence of skewed X chromosome inactivation pattern in a group of mosaic turner syndrome patients. 2016, Anais.. Ribeirão Preto: FMRP-USP, 2016. . Acesso em: 05 nov. 2024.
APA
Ruiz-Lara, G. V., Luchiari, H. R., Galerani, M. V., Huber, J., Machado, F. B., & Ramos, E. S. (2016). Prevalence of skewed X chromosome inactivation pattern in a group of mosaic turner syndrome patients. In Abstracts. Ribeirão Preto: FMRP-USP.
NLM
Ruiz-Lara GV, Luchiari HR, Galerani MV, Huber J, Machado FB, Ramos ES. Prevalence of skewed X chromosome inactivation pattern in a group of mosaic turner syndrome patients. Abstracts. 2016 ;[citado 2024 nov. 05 ]
Vancouver
Ruiz-Lara GV, Luchiari HR, Galerani MV, Huber J, Machado FB, Ramos ES. Prevalence of skewed X chromosome inactivation pattern in a group of mosaic turner syndrome patients. Abstracts. 2016 ;[citado 2024 nov. 05 ]
Trabalho de evento-resumo
Next generation sequencing as a confirmatory diagnostic tool in a Brazilian Skeletal Dysplasia Tertiary Center (2016)
Baratela, W. A. R.; Yamamoto, G. L.; Testai, L. C.; Honjo, R.; Oliveira, L. A. N.; Doriqui, M. J. R.; Rosa, R.; Meira, J. G. C.; Pina Neto, João Monteiro de; Cavalcanti, D. P.; Kim, C. A.; Passos-Bueno, Maria Rita ; Bertola, D. R.
Source: Poster Abstracts. Conference titles: Annual Meeting of the American Society of Human Genetics (ASHG). Unidade: FMRP
Subjects: GENÉTICA MÉDICA, CITOGENÉTICA MOLECULAR
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ABNT
BARATELA, W. A. R. et al. Next generation sequencing as a confirmatory diagnostic tool in a Brazilian Skeletal Dysplasia Tertiary Center. 2016, Anais.. Vancouver: ASHG, 2016. . Acesso em: 05 nov. 2024.
APA
Baratela, W. A. R., Yamamoto, G. L., Testai, L. C., Honjo, R., Oliveira, L. A. N., Doriqui, M. J. R., et al. (2016). Next generation sequencing as a confirmatory diagnostic tool in a Brazilian Skeletal Dysplasia Tertiary Center. In Poster Abstracts. Vancouver: ASHG.
NLM
Baratela WAR, Yamamoto GL, Testai LC, Honjo R, Oliveira LAN, Doriqui MJR, Rosa R, Meira JGC, Pina Neto JM de, Cavalcanti DP, Kim CA, Passos-Bueno MR, Bertola DR. Next generation sequencing as a confirmatory diagnostic tool in a Brazilian Skeletal Dysplasia Tertiary Center. Poster Abstracts. 2016 ;[citado 2024 nov. 05 ]
Vancouver
Baratela WAR, Yamamoto GL, Testai LC, Honjo R, Oliveira LAN, Doriqui MJR, Rosa R, Meira JGC, Pina Neto JM de, Cavalcanti DP, Kim CA, Passos-Bueno MR, Bertola DR. Next generation sequencing as a confirmatory diagnostic tool in a Brazilian Skeletal Dysplasia Tertiary Center. Poster Abstracts. 2016 ;[citado 2024 nov. 05 ]
Trabalho de evento-resumo periodico
Copy-neutral loss of heterozygosity pattern in systemic lupus erythematosus (2015)
Barbosa, Fernanda Bueno; Simioni, Milena; Torres, Fábio Rossi; Donadi, Eduardo Antônio; Gil-da-Silva-Lopes, Vera Lúcia; Simões, Aguinaldo Luiz
Source: Chromosome Research. Conference titles: European Cytogenetics Conference. Unidade: FMRP
Subjects: LÚPUS ERITEMATOSO SISTÊMICO, CITOGENÉTICA MOLECULAR
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ABNT
BARBOSA, Fernanda Bueno et al. Copy-neutral loss of heterozygosity pattern in systemic lupus erythematosus. Chromosome Research. Dordrecht: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. Disponível em: https://doi.org/10.1007/s10577-015-9476-6. Acesso em: 05 nov. 2024. , 2015
APA
Barbosa, F. B., Simioni, M., Torres, F. R., Donadi, E. A., Gil-da-Silva-Lopes, V. L., & Simões, A. L. (2015). Copy-neutral loss of heterozygosity pattern in systemic lupus erythematosus. Chromosome Research. Dordrecht: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. doi:10.1007/s10577-015-9476-6
NLM
Barbosa FB, Simioni M, Torres FR, Donadi EA, Gil-da-Silva-Lopes VL, Simões AL. Copy-neutral loss of heterozygosity pattern in systemic lupus erythematosus [Internet]. Chromosome Research. 2015 ; 23 S38.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1007/s10577-015-9476-6
Vancouver
Barbosa FB, Simioni M, Torres FR, Donadi EA, Gil-da-Silva-Lopes VL, Simões AL. Copy-neutral loss of heterozygosity pattern in systemic lupus erythematosus [Internet]. Chromosome Research. 2015 ; 23 S38.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1007/s10577-015-9476-6
Trabalho de evento-resumo
Genome-wide copy number variation analysis in systemic lupus erythematosus (2015)
Barbosa, F. B; Simioni, M; Torres, F. R; Donadi, Eduardo Antônio; Gil-da-Silva-Lopes, V. L; Simões, Aguinaldo Luiz
Source: Abstracts. Conference titles: European Human Genetics Conference. Unidade: FMRP
Subjects: LÚPUS ERITEMATOSO SISTÊMICO, CITOGENÉTICA MOLECULAR
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ABNT
BARBOSA, F. B et al. Genome-wide copy number variation analysis in systemic lupus erythematosus. 2015, Anais.. Glasgow: ESHG, 2015. . Acesso em: 05 nov. 2024.
APA
Barbosa, F. B., Simioni, M., Torres, F. R., Donadi, E. A., Gil-da-Silva-Lopes, V. L., & Simões, A. L. (2015). Genome-wide copy number variation analysis in systemic lupus erythematosus. In Abstracts. Glasgow: ESHG.
NLM
Barbosa FB, Simioni M, Torres FR, Donadi EA, Gil-da-Silva-Lopes VL, Simões AL. Genome-wide copy number variation analysis in systemic lupus erythematosus. Abstracts. 2015 ;[citado 2024 nov. 05 ]
Vancouver
Barbosa FB, Simioni M, Torres FR, Donadi EA, Gil-da-Silva-Lopes VL, Simões AL. Genome-wide copy number variation analysis in systemic lupus erythematosus. Abstracts. 2015 ;[citado 2024 nov. 05 ]
Artigo de periodico
Subtelomeric 6p25 deletion/duplication: report of a patient with new clinical findings and genotype–phenotype correlations (2015)
Linhares, Natália D; Svartman, Marta; Rodrigues, Tatiane C; Rosenberg, Carla ; Valadares, Eugênia R
Source: European Journal of Medical Genetics. Unidade: IB
Subjects: GENÓTIPOS, FENÓTIPOS, GENOMAS, PROTEÍNAS, GENÉTICA MÉDICA, CITOGENÉTICA MOLECULAR
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ABNT
LINHARES, Natália D et al. Subtelomeric 6p25 deletion/duplication: report of a patient with new clinical findings and genotype–phenotype correlations. European Journal of Medical Genetics, v. 58, n. 5, p. 310-318, 2015Tradução . . Disponível em: https://doi.org/10.1016/j.ejmg.2015.02.011. Acesso em: 05 nov. 2024.
APA
Linhares, N. D., Svartman, M., Rodrigues, T. C., Rosenberg, C., & Valadares, E. R. (2015). Subtelomeric 6p25 deletion/duplication: report of a patient with new clinical findings and genotype–phenotype correlations. European Journal of Medical Genetics, 58( 5), 310-318. doi:10.1016/j.ejmg.2015.02.011
NLM
Linhares ND, Svartman M, Rodrigues TC, Rosenberg C, Valadares ER. Subtelomeric 6p25 deletion/duplication: report of a patient with new clinical findings and genotype–phenotype correlations [Internet]. European Journal of Medical Genetics. 2015 ; 58( 5): 310-318.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1016/j.ejmg.2015.02.011
Vancouver
Linhares ND, Svartman M, Rodrigues TC, Rosenberg C, Valadares ER. Subtelomeric 6p25 deletion/duplication: report of a patient with new clinical findings and genotype–phenotype correlations [Internet]. European Journal of Medical Genetics. 2015 ; 58( 5): 310-318.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1016/j.ejmg.2015.02.011
Artigo de periodico
Investigation of selected genomic deletions and duplications in a cohort of 338 patients presenting with syndromic obesity by multiplex ligation-dependent probe amplification using synthetic probes (2014)
D'Angelo, Carla Sustek; Varela, Monica C; Castro, Claudia I. E. de; Kim, Chong Ae; Bertola, Débora Romeo; Lourenço, Charles Marques; Perez, Ana Beatriz A; Koiffmann, Celia Priszkulnik
Source: Molecular Cytogenetics. Unidades: IB, FM
Subjects: DELEÇÃO DE GENES, DEFICIÊNCIA MENTAL, OBESIDADE, CITOGENÉTICA MOLECULAR, GENÉTICA MÉDICA
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ABNT
D'ANGELO, Carla Sustek et al. Investigation of selected genomic deletions and duplications in a cohort of 338 patients presenting with syndromic obesity by multiplex ligation-dependent probe amplification using synthetic probes. Molecular Cytogenetics, v. 7, n. 1, p. 1-13, 2014Tradução . . Disponível em: https://doi.org/10.1186/s13039-014-0075-6. Acesso em: 05 nov. 2024.
APA
D'Angelo, C. S., Varela, M. C., Castro, C. I. E. de, Kim, C. A., Bertola, D. R., Lourenço, C. M., et al. (2014). Investigation of selected genomic deletions and duplications in a cohort of 338 patients presenting with syndromic obesity by multiplex ligation-dependent probe amplification using synthetic probes. Molecular Cytogenetics, 7( 1), 1-13. doi:10.1186/s13039-014-0075-6
NLM
D'Angelo CS, Varela MC, Castro CIE de, Kim CA, Bertola DR, Lourenço CM, Perez ABA, Koiffmann CP. Investigation of selected genomic deletions and duplications in a cohort of 338 patients presenting with syndromic obesity by multiplex ligation-dependent probe amplification using synthetic probes [Internet]. Molecular Cytogenetics. 2014 ; 7( 1): 1-13.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1186/s13039-014-0075-6
Vancouver
D'Angelo CS, Varela MC, Castro CIE de, Kim CA, Bertola DR, Lourenço CM, Perez ABA, Koiffmann CP. Investigation of selected genomic deletions and duplications in a cohort of 338 patients presenting with syndromic obesity by multiplex ligation-dependent probe amplification using synthetic probes [Internet]. Molecular Cytogenetics. 2014 ; 7( 1): 1-13.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1186/s13039-014-0075-6
Artigo de periodico
Biogeographic patterns in the chromosomal distribution of a satellite DNA in the banded tetra Astyanax fasciatus (Teleostei: Characiformes) (2013)
Kavalco, Karine Frehner; Pazza, Rubens; Brandão, Karina de Oliveira; Almeida-Toledo, Lurdes Foresti de
Source: Organisms Diversity & Evolution. Unidade: IB
Subjects: CITOGENÉTICA MOLECULAR, SEQUÊNCIA DO DNA, CHARACIFORMES, OSTEICHTHYES
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ABNT
KAVALCO, Karine Frehner et al. Biogeographic patterns in the chromosomal distribution of a satellite DNA in the banded tetra Astyanax fasciatus (Teleostei: Characiformes). Organisms Diversity & Evolution, v. 13, n. 1, p. 67-76, 2013Tradução . . Disponível em: https://doi.org/10.1007/s13127-012-0100-8. Acesso em: 05 nov. 2024.
APA
Kavalco, K. F., Pazza, R., Brandão, K. de O., & Almeida-Toledo, L. F. de. (2013). Biogeographic patterns in the chromosomal distribution of a satellite DNA in the banded tetra Astyanax fasciatus (Teleostei: Characiformes). Organisms Diversity & Evolution, 13( 1), 67-76. doi:10.1007/s13127-012-0100-8
NLM
Kavalco KF, Pazza R, Brandão K de O, Almeida-Toledo LF de. Biogeographic patterns in the chromosomal distribution of a satellite DNA in the banded tetra Astyanax fasciatus (Teleostei: Characiformes) [Internet]. Organisms Diversity & Evolution. 2013 ; 13( 1): 67-76.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1007/s13127-012-0100-8
Vancouver
Kavalco KF, Pazza R, Brandão K de O, Almeida-Toledo LF de. Biogeographic patterns in the chromosomal distribution of a satellite DNA in the banded tetra Astyanax fasciatus (Teleostei: Characiformes) [Internet]. Organisms Diversity & Evolution. 2013 ; 13( 1): 67-76.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1007/s13127-012-0100-8
Trabalho de evento-resumo
Is Colombian Anastrepha fraterculus S. l. a different species?: citogenetical and genetical evidence (2012)
Canal, Nelson A; Carranza, Juilo Cesar; Castañeda, Maria del Rosario; Zabala, Daniel; Selivon, Denise ; Perondini, André Luiz Paranhos
Source: Abstract. Conference titles: Research Coordination Meeting (CRP). Unidade: IB
Subjects: MOSCA-DAS-FRUTAS, CITOGENÉTICA MOLECULAR
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ABNT
CANAL, Nelson A et al. Is Colombian Anastrepha fraterculus S. l. a different species?: citogenetical and genetical evidence. 2012, Anais.. Brisbane: Instituto de Biociências, Universidade de São Paulo, 2012. . Acesso em: 05 nov. 2024.
APA
Canal, N. A., Carranza, J. C., Castañeda, M. del R., Zabala, D., Selivon, D., & Perondini, A. L. P. (2012). Is Colombian Anastrepha fraterculus S. l. a different species?: citogenetical and genetical evidence. In Abstract. Brisbane: Instituto de Biociências, Universidade de São Paulo.
NLM
Canal NA, Carranza JC, Castañeda M del R, Zabala D, Selivon D, Perondini ALP. Is Colombian Anastrepha fraterculus S. l. a different species?: citogenetical and genetical evidence. Abstract. 2012 ;[citado 2024 nov. 05 ]
Vancouver
Canal NA, Carranza JC, Castañeda M del R, Zabala D, Selivon D, Perondini ALP. Is Colombian Anastrepha fraterculus S. l. a different species?: citogenetical and genetical evidence. Abstract. 2012 ;[citado 2024 nov. 05 ]
Trabalho de evento-resumo
Molecular cytogenetics characterization of an apparently balanced translocation (X;22) associated with infertility (2012)
Grzesiuk, J. D.; Pereira, C. S.; Huber, J.; Santos, S. A.; Martelli, Lúcia Regina
Source: Resumos. Conference titles: Workshop do Programa de Pós-Graduação em Genética da FMRP-USP. Unidade: FMRP
Subjects: CITOGENÉTICA MOLECULAR, DOENÇAS GENÉTICAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GRZESIUK, J. D. et al. Molecular cytogenetics characterization of an apparently balanced translocation (X;22) associated with infertility. 2012, Anais.. Ribeirão Preto: FMRP-USP, 2012. . Acesso em: 05 nov. 2024.
APA
Grzesiuk, J. D., Pereira, C. S., Huber, J., Santos, S. A., & Martelli, L. R. (2012). Molecular cytogenetics characterization of an apparently balanced translocation (X;22) associated with infertility. In Resumos. Ribeirão Preto: FMRP-USP.
NLM
Grzesiuk JD, Pereira CS, Huber J, Santos SA, Martelli LR. Molecular cytogenetics characterization of an apparently balanced translocation (X;22) associated with infertility. Resumos. 2012 ;[citado 2024 nov. 05 ]
Vancouver
Grzesiuk JD, Pereira CS, Huber J, Santos SA, Martelli LR. Molecular cytogenetics characterization of an apparently balanced translocation (X;22) associated with infertility. Resumos. 2012 ;[citado 2024 nov. 05 ]
Artigo de periodico
Comparative cytogenetics and molecular phylogeography in the group Astyanax altiparanae – Astyanax aff. bimaculatus (Teleostei, Characidae) (2011)
Kavalco, Karine Frehner; Pazza, Rubens; Brandão, K. O; Garcia, C; Almeida-Toledo, Lurdes Foresti de
Source: Cytogenetic and Genome Research. Unidade: IB
Subjects: CITOGENÉTICA MOLECULAR, OSTEICHTHYES, CHARACIFORMES, FILOGENIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
KAVALCO, Karine Frehner et al. Comparative cytogenetics and molecular phylogeography in the group Astyanax altiparanae – Astyanax aff. bimaculatus (Teleostei, Characidae). Cytogenetic and Genome Research, v. 134, n. 2, p. 108-119, 2011Tradução . . Disponível em: https://doi.org/10.1159/000325539. Acesso em: 05 nov. 2024.
APA
Kavalco, K. F., Pazza, R., Brandão, K. O., Garcia, C., & Almeida-Toledo, L. F. de. (2011). Comparative cytogenetics and molecular phylogeography in the group Astyanax altiparanae – Astyanax aff. bimaculatus (Teleostei, Characidae). Cytogenetic and Genome Research, 134( 2), 108-119. doi:10.1159/000325539
NLM
Kavalco KF, Pazza R, Brandão KO, Garcia C, Almeida-Toledo LF de. Comparative cytogenetics and molecular phylogeography in the group Astyanax altiparanae – Astyanax aff. bimaculatus (Teleostei, Characidae) [Internet]. Cytogenetic and Genome Research. 2011 ; 134( 2): 108-119.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1159/000325539
Vancouver
Kavalco KF, Pazza R, Brandão KO, Garcia C, Almeida-Toledo LF de. Comparative cytogenetics and molecular phylogeography in the group Astyanax altiparanae – Astyanax aff. bimaculatus (Teleostei, Characidae) [Internet]. Cytogenetic and Genome Research. 2011 ; 134( 2): 108-119.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1159/000325539
Artigo de periodico
Molecular cytogenetics of Astyanax ribeirae (Teleostei, Characidae), an endemic characin of the Atlantic rainforest (2010)
Kavalco, Karine Frehner; Pazza, Rubens; Almeida-Toledo, Lurdes Foresti de
Source: The Nucleus. Unidade: IB
Subjects: GENÉTICA ECOLÓGICA, CHARACIFORMES, CITOGENÉTICA (ANÁLISE), CITOGENÉTICA MOLECULAR
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
KAVALCO, Karine Frehner e PAZZA, Rubens e ALMEIDA-TOLEDO, Lurdes Foresti de. Molecular cytogenetics of Astyanax ribeirae (Teleostei, Characidae), an endemic characin of the Atlantic rainforest. The Nucleus, v. 53, n. 1-2, p. 51-54, 2010Tradução . . Disponível em: https://doi.org/10.1007/s13237-010-0006-9. Acesso em: 05 nov. 2024.
APA
Kavalco, K. F., Pazza, R., & Almeida-Toledo, L. F. de. (2010). Molecular cytogenetics of Astyanax ribeirae (Teleostei, Characidae), an endemic characin of the Atlantic rainforest. The Nucleus, 53( 1-2), 51-54. doi:10.1007/s13237-010-0006-9
NLM
Kavalco KF, Pazza R, Almeida-Toledo LF de. Molecular cytogenetics of Astyanax ribeirae (Teleostei, Characidae), an endemic characin of the Atlantic rainforest [Internet]. The Nucleus. 2010 ; 53( 1-2): 51-54.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1007/s13237-010-0006-9
Vancouver
Kavalco KF, Pazza R, Almeida-Toledo LF de. Molecular cytogenetics of Astyanax ribeirae (Teleostei, Characidae), an endemic characin of the Atlantic rainforest [Internet]. The Nucleus. 2010 ; 53( 1-2): 51-54.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1007/s13237-010-0006-9
Artigo de periodico
Comparative chromosomal analyses in species of the genus Pimelodella (Siluriformes, Heptapteridae): occurrence of structural and numerical polymorphisms (2010)
Garcia, Caroline; Almeida-Toledo, Lurdes Foresti de
Source: Caryologia. Unidade: IB
Subjects: POLIMORFISMO, CROMOSSOMOS SEXUAIS, SILURIFORMES, CITOGENÉTICA MOLECULAR
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GARCIA, Caroline e ALMEIDA-TOLEDO, Lurdes Foresti de. Comparative chromosomal analyses in species of the genus Pimelodella (Siluriformes, Heptapteridae): occurrence of structural and numerical polymorphisms. Caryologia, v. 63, n. 1, p. 32-40, 2010Tradução . . Disponível em: https://doi.org/10.1080/00087114.2010.10589706. Acesso em: 05 nov. 2024.
APA
Garcia, C., & Almeida-Toledo, L. F. de. (2010). Comparative chromosomal analyses in species of the genus Pimelodella (Siluriformes, Heptapteridae): occurrence of structural and numerical polymorphisms. Caryologia, 63( 1), 32-40. doi:10.1080/00087114.2010.10589706
NLM
Garcia C, Almeida-Toledo LF de. Comparative chromosomal analyses in species of the genus Pimelodella (Siluriformes, Heptapteridae): occurrence of structural and numerical polymorphisms [Internet]. Caryologia. 2010 ; 63( 1): 32-40.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1080/00087114.2010.10589706
Vancouver
Garcia C, Almeida-Toledo LF de. Comparative chromosomal analyses in species of the genus Pimelodella (Siluriformes, Heptapteridae): occurrence of structural and numerical polymorphisms [Internet]. Caryologia. 2010 ; 63( 1): 32-40.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1080/00087114.2010.10589706
Artigo de periodico
Cryptic SYT/SXX1 fusion gene in high-grade biphasic synovial sarcoma with unique complex rearrangement and extensice BCL2 overexpression (2010)
Brassesco, María Sol; Cortez, Maria Angélica; Valera, Elvis Terci; Engel, Edgard Eduard; Barbosa, Marcello Henrique Nogueira; Becker, Aline Paixão; Scrideli, Carlos Alberto; Tone, Luiz Gonzaga
Source: Cancer Genetics and Cytogenetics. Unidade: FMRP
Subjects: CITOGENÉTICA MOLECULAR, SARCOMA, MULHERES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BRASSESCO, María Sol et al. Cryptic SYT/SXX1 fusion gene in high-grade biphasic synovial sarcoma with unique complex rearrangement and extensice BCL2 overexpression. Cancer Genetics and Cytogenetics, v. 196, n. 2, p. 189-193, 2010Tradução . . Disponível em: https://doi.org/10.1016/j.cancergencyto.2009.10.001. Acesso em: 05 nov. 2024.
APA
Brassesco, M. S., Cortez, M. A., Valera, E. T., Engel, E. E., Barbosa, M. H. N., Becker, A. P., et al. (2010). Cryptic SYT/SXX1 fusion gene in high-grade biphasic synovial sarcoma with unique complex rearrangement and extensice BCL2 overexpression. Cancer Genetics and Cytogenetics, 196( 2), 189-193. doi:10.1016/j.cancergencyto.2009.10.001
NLM
Brassesco MS, Cortez MA, Valera ET, Engel EE, Barbosa MHN, Becker AP, Scrideli CA, Tone LG. Cryptic SYT/SXX1 fusion gene in high-grade biphasic synovial sarcoma with unique complex rearrangement and extensice BCL2 overexpression [Internet]. Cancer Genetics and Cytogenetics. 2010 ; 196( 2): 189-193.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1016/j.cancergencyto.2009.10.001
Vancouver
Brassesco MS, Cortez MA, Valera ET, Engel EE, Barbosa MHN, Becker AP, Scrideli CA, Tone LG. Cryptic SYT/SXX1 fusion gene in high-grade biphasic synovial sarcoma with unique complex rearrangement and extensice BCL2 overexpression [Internet]. Cancer Genetics and Cytogenetics. 2010 ; 196( 2): 189-193.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1016/j.cancergencyto.2009.10.001

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